Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121